食品科学

• 营养卫生 • 上一篇    下一篇

高脂饮食对菌群人源化小鼠肠道菌群结构的影响

陈杏云1,曾本华2,魏 泓2,胡新中1,3,*   

  1. 1.西北农林科技大学食品科学与工程学院,陕西 杨凌 712100;2.第三军医大学基础部实验动物学教研室,重庆 400038;
    3.陕西师范大学食品工程与营养科学学院,陕西 西安 710062
  • 出版日期:2013-09-15 发布日期:2013-09-27
  • 通讯作者: 胡新中
  • 基金资助:

    国家燕麦荞麦产业技术体系建设项目(CARS-08-D1);陕西省国际合作项目(2011KW-28);
    国家“973”计划项目(2013CB531406);西北农林科技大学国际平台项目

Effect of High-fat Diet on the Structure of Gut Microbiota in Human Flora-associated Mice

CHEN Xing-yun1,ZENG Ben-hua2,WEI Hong2,HU Xin-zhong1,3,*   

  1. 1. College of Food Science and Engineering, Northwest A&F University, Yangling 712100, China;2. Department of Laboratory
    Animal Science, College of Basic Medical Sciences, Third Military Medical University, Chongqing 400038, China;
    3. College of Food Engineering and Nutritional Science, Shaanxi Normal University, Xi’an 710062, China
  • Online:2013-09-15 Published:2013-09-27
  • Contact: HU Xin-zhong

摘要:

采用高脂饮食建立肥胖菌群人源化(HFA)小鼠模型,研究高脂饮食对HFA小鼠肠道微生态结构的影响,探讨肥胖、饮食与肠道菌群之间的关系。将20只无菌小鼠接种健康人志愿者的粪便悬液构建HFA小鼠模型后分为普通组和高脂组,分别用基础饲料和高脂饲料饲喂8周,测定小鼠体质量、血糖血脂以及用PCR-DGGE方法检测肠道菌群的变化。结果显示:与普通组HFA小鼠相比,高脂组HFA小鼠体质量、肝质量、脂肪组织质量及血清中总甘油三酯水平显著增加(P<0.01),血糖水平也显著增加(P<0.05)。同时高脂组HFA小鼠肠道微生物多样性指数显著升高(P<0.05),正常优势菌群丰度降低,零时刻时的非优势菌群丰度增加,测序结果表明高脂饮食可能会诱导HFA小鼠肠道Staphylococcus lentus、Staphylococcus vitulinus和Shigella flexneri等有害菌生长繁殖。本实验采用高脂饮食成功建立起肥胖HFA小鼠模型并证实了高脂饮食明显改变HFA小鼠肠道菌群结构。肠道菌群组成和细菌丰度发生很大变化导致肠道微生态失调,这提示人源性肠道菌群可能参与饮食结构失衡引起的肥胖的发展。

关键词: 无菌小鼠, 菌群人源化小鼠, 肠道菌群, 高脂饮食, 肥胖, PCR-DGGE

Abstract:

In order to explore the relationship among diet, obesity and intestinal microbiota, high-fat diet was used to
establish obese human flora-associated (HFA) mouse model to investigate the effect of high fat diet on the structure of
gut microbiota in HFA mice. Totally 20 pathogen-free mice were inoculated with fecal suspension derived from a healthy
volunteer to obtain HFA mice. The HFA mice were fed a control or a high-fat diet for 8 weeks. Body weight, blood glucose
and blood fat were determined and the change in gut microbiota was analyzed by PCR-DGGE. Results showed that body
weight, liver weight, fat tissue weight and serum total triglyceride level revealed a significant increase (P < 0.01) in the
high-fat group when compared with the control group. Blood glucose level also increased significantly (P < 0.05) in highfat
diet-fed HFA mice. The gut bacterial diversity index of the high-fat group significantly increased (P < 0.05). The
abundance of the dominant bacteria at zero time reduced, but the abundance of bacteria that were not dominant at zero time
increased. DNA sequencing showed that high-fat diet may induce Staphylococcus lentus, Staphylococcus vitulinus and
Shigella flexneri to bloom in the gut of HFA mice. An obese HFA mouse model was successfully established by feeding a
high-fat diet and high-fat diet obviously altered the structure of gut microbiota in HFA mice. The composition and bacterial
abundance of intestinal flora in high-fat diet-feed HFA mice greatly changed, leading to intestinal dysbacteriosis. It suggests
that human-derived intestinal flora may be involved in the development of obesity caused by imbalanced dietary profile.

Key words: pathogen-free mice, human flora-associated mice, gut microbiota, high-fat diet, obesity, PCR-DGGE

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